Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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Affected kits of drb1*11 ssp unitray produce a false negative in lane 11 in the presence of drb1*1165. a laboratory would be unable to identify the sample as a drb1*1165.